drugset / Trial / NCT00526136
Vernakalant (Oral) Prevention of Atrial Fibrillation Recurrence Post-Conversion Study
RandomizedParallel-groupDouble-blindPrevention
Summary
To evaluate the safety, tolerability and efficacy of 3 doses of vernakalant (oral) (150 mg, 300 mg and 500 mg b.i.d.) administered for up to 90 days in subjects with sustained symptomatic atrial fibrillation (AF duration \> 72 hours and \< 6 months).
Timeline
- Start
- 2007-03
- Primary completion
- —
- Completion
- 2008-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vernakalant | Other / unclassified | 150 mg | Oral |
| Subject | Vernakalant | Other / unclassified | 300 mg | Oral |
| Subject | Vernakalant | Other / unclassified | 500 mg | Oral |